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Analyze Cancer Data in Just a Few Clicks

Saphyr Cancer Circos Data

Take complex, time-consuming bioinformatics out of your process and discover new critical insights about your cancer research samples in minutes with Saphyr® Optical Genome Mapping and Bionano Access® software.

Analyze all the structural variants including complex rearrangements with highly sensitive SV detection down to 1% allele fraction.

Intuitive, best-in-class data visualization and automated analysis tools significantly reduce your costs per sample and time to results to accelerate the translation of new ideas into the clinic.

Bionano’s technology provides oncologists with a global view of somatic SVs across the entire tumor genome with a 10,000 times greater resolution than karyotyping. We anticipate that OGM will yield unprecedented insights into solid and liquid tumors, with the potential for a steady improvement in diagnosis, treatment, and thus improved patient outcomes.

James R. Broach
Director, Penn State Institute for Personalized Medicine

Save time and reveal more with Saphyr and Bionano Access

Perform true genome-wide SV analysis in human or mouse free from amplification bias and the limitations of panels
Visualize entire genomes with interactive circos plots and get a deeper understanding of your samples at a glance
Identify somatic SVs fast with a one-click filter that removes population variation using our built-in control database

See what Saphyr can do for you


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